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In Vivo Flow Cytometry of Extremely Rare Circulating Cells
Circulating tumor cells (CTCs) are of great interest in cancer research, but methods for their enumeration remain far from optimal. We developed a new small animal research tool called “Diffuse in vivo Flow Cytometry” (DiFC) for detecting extremely rare fluorescently-labeled circulating cells direct...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399281/ https://www.ncbi.nlm.nih.gov/pubmed/30833671 http://dx.doi.org/10.1038/s41598-019-40143-2 |
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author | Tan, Xuefei Patil, Roshani Bartosik, Peter Runnels, Judith M. Lin, Charles P. Niedre, Mark |
author_facet | Tan, Xuefei Patil, Roshani Bartosik, Peter Runnels, Judith M. Lin, Charles P. Niedre, Mark |
author_sort | Tan, Xuefei |
collection | PubMed |
description | Circulating tumor cells (CTCs) are of great interest in cancer research, but methods for their enumeration remain far from optimal. We developed a new small animal research tool called “Diffuse in vivo Flow Cytometry” (DiFC) for detecting extremely rare fluorescently-labeled circulating cells directly in the bloodstream. The technique exploits near-infrared diffuse photons to detect and count cells flowing in large superficial arteries and veins without drawing blood samples. DiFC uses custom-designed, dual fiber optic probes that are placed in contact with the skin surface approximately above a major vascular bundle. In combination with a novel signal processing algorithm, DiFC allows counting of individual cells moving in arterial or venous directions, as well as measurement of their speed and depth. We show that DiFC allows sampling of the entire circulating blood volume of a mouse in under 10 minutes, while maintaining a false alarm rate of 0.014 per minute. In practice, this means that DiFC allows reliable detection of circulating cells below 1 cell per mL. Hence, the unique capabilities of DiFC are highly suited to biological applications involving very rare cell types such as the study of hematogenous cancer metastasis. |
format | Online Article Text |
id | pubmed-6399281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63992812019-03-07 In Vivo Flow Cytometry of Extremely Rare Circulating Cells Tan, Xuefei Patil, Roshani Bartosik, Peter Runnels, Judith M. Lin, Charles P. Niedre, Mark Sci Rep Article Circulating tumor cells (CTCs) are of great interest in cancer research, but methods for their enumeration remain far from optimal. We developed a new small animal research tool called “Diffuse in vivo Flow Cytometry” (DiFC) for detecting extremely rare fluorescently-labeled circulating cells directly in the bloodstream. The technique exploits near-infrared diffuse photons to detect and count cells flowing in large superficial arteries and veins without drawing blood samples. DiFC uses custom-designed, dual fiber optic probes that are placed in contact with the skin surface approximately above a major vascular bundle. In combination with a novel signal processing algorithm, DiFC allows counting of individual cells moving in arterial or venous directions, as well as measurement of their speed and depth. We show that DiFC allows sampling of the entire circulating blood volume of a mouse in under 10 minutes, while maintaining a false alarm rate of 0.014 per minute. In practice, this means that DiFC allows reliable detection of circulating cells below 1 cell per mL. Hence, the unique capabilities of DiFC are highly suited to biological applications involving very rare cell types such as the study of hematogenous cancer metastasis. Nature Publishing Group UK 2019-03-04 /pmc/articles/PMC6399281/ /pubmed/30833671 http://dx.doi.org/10.1038/s41598-019-40143-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tan, Xuefei Patil, Roshani Bartosik, Peter Runnels, Judith M. Lin, Charles P. Niedre, Mark In Vivo Flow Cytometry of Extremely Rare Circulating Cells |
title | In Vivo Flow Cytometry of Extremely Rare Circulating Cells |
title_full | In Vivo Flow Cytometry of Extremely Rare Circulating Cells |
title_fullStr | In Vivo Flow Cytometry of Extremely Rare Circulating Cells |
title_full_unstemmed | In Vivo Flow Cytometry of Extremely Rare Circulating Cells |
title_short | In Vivo Flow Cytometry of Extremely Rare Circulating Cells |
title_sort | in vivo flow cytometry of extremely rare circulating cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399281/ https://www.ncbi.nlm.nih.gov/pubmed/30833671 http://dx.doi.org/10.1038/s41598-019-40143-2 |
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